Affiliation:
1. Department of Microbiology, Tufts University School of Medicine, and Howard Hughes Medical Institute, Boston, Massachusetts
Abstract
ABSTRACT
Transfer of SXT, a
Vibrio cholerae
-derived integrating conjugative element that encodes multiple antibiotic resistance genes, is repressed by SetR, a λ
434
c
I-related repressor. Here we identify divergent promoters between
s086
and
setR
that drive expression of the regulators of SXT transfer. One transcript encodes the activators of transfer,
setC
and
setD
. The second transcript codes for SetR and, like the
c
I transcript of lambda, is leaderless. SetR binds to four operators located between
setR
and
s086
; the locations and relative affinities of these sites suggest a model for regulation of SXT transfer.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
45 articles.
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